EP2166875A1 - Verfahren zur entfernung von essiggeruch - Google Patents
Verfahren zur entfernung von essiggeruchInfo
- Publication number
- EP2166875A1 EP2166875A1 EP08760582A EP08760582A EP2166875A1 EP 2166875 A1 EP2166875 A1 EP 2166875A1 EP 08760582 A EP08760582 A EP 08760582A EP 08760582 A EP08760582 A EP 08760582A EP 2166875 A1 EP2166875 A1 EP 2166875A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- vinegar
- odor
- acid
- lactate
- ethyl acetate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12J—VINEGAR; PREPARATION OR PURIFICATION THEREOF
- C12J1/00—Vinegar; Preparation or purification thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
- A23L5/27—Removal of unwanted matter, e.g. deodorisation or detoxification by chemical treatment, by adsorption or by absorption
- A23L5/276—Treatment with inorganic compounds
Definitions
- the invention pertains to a method for removing odor from vinegar.
- Vinegar is a blend of acids comprising acetic acid.
- a recurrent problem of vinegar is its glue/solvent-like odor, which is attributed to the presence of ethyl acetate, which is an impurity that is naturally present in vinegar.
- Ethyl acetate is formed by esterification of acetic acid and ethanol which both are present in vinegar obtained from fermentation processes .
- Various methods have been proposed for the removal of ethyl acetate from vinegar. In JP 7075543 raw vinegar having a temperature of 40-70 0 C was brought into contact with a gaseous phase reduced into an atmospheric pressure of 60-160 mmHg to remove volatile substances.
- JP 3123480 vinegar originating from cereals, fruits and/or sugars was brought into contact with a nonionic porous synthetic adsorbent, thereby adsorbing and removing ill-odor substances existing in the vinegar.
- This method was not primarily aimed at the removal of ethyl acetate, but at the removal of isovaleric acid and phenylacetic acid.
- JP 60137281 the vinegar having ill odor and taste was blasted with steam pressurized to a pressure sufficient to cause the elimination of the ill-odor.
- the latter is of importance because vinegar is sold for treating meat or for making dressings, and the vinegar can be shelved for several months prior to its use.
- Such improved method for removing odor and maintaining taste from vinegar comprises: a) increasing the pH of the vinegar with base to at least 6; b) maintaining said pH for at least 15 minutes at 40-90 0 C; c) adding acid to obtain vinegar having pH between 6 and 8, if the pH of the vinegar of step b) is 8 or higher.
- step a) the pH is increased with base.
- base in principle any base can be used, but alkali metal base is preferred, particularly potassium or sodium hydroxide. Mixtures of bases can also be used.
- the pH is increased to at least 6, but for increasing the reaction rate a pH of at least 8, preferably at least 9.5 is favored. Typically, pH of about 10 has been found very suitable and effective.
- An important additive contribution to the process may be the evaporation of at least part of the volatile constituents during or after step b) .
- These constituents may be ethyl acetate, but other volatile ill-odor products such as isovaleric acid and phenyl acetic acid are removed as well.
- the evaporation is not necessary but can further improve the process. Evaporation already occurs at room temperature, but this needs relatively long process times.
- the vinegar is preferably heated to 40-90 0 C, more preferably to 50-80 0 C, which is sufficiently high to evaporate ethyl acetate, possibly as an azeotropic mixture with water, and low enough to prevent deterioration of the vinegar.
- evaporation is performed under reduced pressure to speed up the process.
- a standing time of about 1 hour at 60 0 C is sufficient to fully remove ethyl acetate. Shorter times up to 15 minutes are possible, particularly when using higher temperatures. When using lower temperatures usually longer times are required.
- a standing time of 2 hours is usually sufficient to fully remove the odor. It is generally not necessary to apply standing times longer than 24 hours, but longer standing times do not harm the process.
- the evaporation process, if applied, can be supported by stirring the vinegar and/or distilling the volatile products.
- the vinegar is brought again to acidic or neutral pH by adding acid, if the vinegar has a pH higher than 8. Commonly this step is performed after cooling the vinegar to about room temperature, if elevated temperatures were used during the standing and/or evaporation. Acids can be added such as malic acid, acetic acid, propionic acid, citric acid, tartaric acid, and lactic acid. Adding hydroxy acids is preferred, and lactic acid, citric acid, or mixtures thereof have the greatest preference.
- the pH is thereby brought to below pH 8, typically to about pH 6 to 8 to obtain so-called neutralized vinegar, which is used as antibacterial agent in the meat industry.
- the method of the invention has in addition to the permanent removal of ill-odor constituents the advantage that the good vinegar taste is maintained.
- the method comprises adding lactate ion. This can be done prior or during step a) . This addition can also be done after step a) but in that case the lactate ion does not contribute to the removal of ill- odor.
- the lactate ion may be added as sodium, ammonium, or potassium lactate, or as a mixture thereof. Most preferably potassium lactate or sodium lactate, or a mixture thereof is added. It can further be of advantage when in addition thereto also sodium and/or potassium hydroxide are added to the vinegar, particularly to bring the pH to the desired value.
- the above method can be combined with any one the prior art methods, such as purging the vinegar with air or steam, or treating the vinegar with an adsorbent or membrane.
- the method of this invention provides vinegar that is stable, which means that ethyl acetate is not longer formed under the neutral conditions during shelving.
- Samples based on commercially available normal vinegar and on commercially available vinegar from which ethyl acetate was removed by the manufacturer were evaluated.
- the composition of the samples comprising a mixture of potassium lactate and commercially available vinegar is given in Table 1.
- the samples were prepared as follows: A beaker glass was filled with potassium lactate (PURASAL® HiPure P Plus, ex Purac) at room temperature and under stirring the vinegar and demineralized water were added. Potassium hydroxide solution was added under stirring and the pH was directly measured at room temperature. The pH was thereafter determined for a 10% water solution by taking 16.7 g of the sample and adding demineralized water to 100 gram, and measuring at room temperature.
- the samples were stored in glass jars and kept in a refrigerator at 0-5 0 C.
- Mixtures based on normal vinegar and on so-marketed flavorless vinegar not having undergone the method of the present invention have almost the same odor profile (solvent, glue, vinegar ⁇ .
- Example 2 Samples according the invention and comparison samples were evaluated.
- the composition of the samples comprising a mixture of vinegar and potassium lactate is given in Table 3.
- Sample III according to the invention was prepared as follows: A beaker glass was filled with 68 g of potassium lactate (PURASAL® HiPure P Plus, ex Purac) at room temperature and under stirring 11 g of vinegar (White distilled 300 grain; ex Fleischmann) and 12 mL of demineralized water were added. 6 g of an aqueous 50% potassium hydroxide solution was added under stirring until a pH of 9.5 was reached (directly measured) . The solution was heated to 60 0 C and kept at this temperature for one hour while stirring. The solution was cooled to room temperature. Lactic acid (PURAC FCC 80, ex Purac) was added until a pH of 6.7 was reached. The samples were stored in glass jars and kept in a refrigerator at 0-5 0 C.
- Sample IV is a blend of potassium lactate and normal vinegar, which was prepared as follows:
- a beaker glass was filled with 72 g of potassium lactate (PURASAL® HiPure P Plus, ex Purac) at room temperature and under stirring 11 g of vinegar (White distilled; ex
- Sample III according to the invention was not found by the sensory panelists to have the disliking solvent/glue-like smell of Sample IV. Analysis further showed that nearly all ethyl acetate and ethanol were removed from Sample III in contrast to sample IV which contained commercially available vinegar and was not treated according to the method of the present invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Food Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Genetics & Genomics (AREA)
- Nutrition Science (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- General Preparation And Processing Of Foods (AREA)
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
- Cereal-Derived Products (AREA)
- Seasonings (AREA)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08760582A EP2166875B1 (de) | 2007-06-07 | 2008-06-05 | Verfahren zur entfernung von essiggeruch |
PL08760582T PL2166875T3 (pl) | 2007-06-07 | 2008-06-05 | Sposób usuwania zapachu z octu |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07109815A EP2000035A1 (de) | 2007-06-07 | 2007-06-07 | Verfahren zur Unterdrückung von Essiggeruch |
PCT/EP2008/057006 WO2008148848A1 (en) | 2007-06-07 | 2008-06-05 | Method for removing odor from vinegar |
EP08760582A EP2166875B1 (de) | 2007-06-07 | 2008-06-05 | Verfahren zur entfernung von essiggeruch |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2166875A1 true EP2166875A1 (de) | 2010-03-31 |
EP2166875B1 EP2166875B1 (de) | 2013-02-27 |
Family
ID=38585857
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07109815A Withdrawn EP2000035A1 (de) | 2007-06-07 | 2007-06-07 | Verfahren zur Unterdrückung von Essiggeruch |
EP08760582A Active EP2166875B1 (de) | 2007-06-07 | 2008-06-05 | Verfahren zur entfernung von essiggeruch |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07109815A Withdrawn EP2000035A1 (de) | 2007-06-07 | 2007-06-07 | Verfahren zur Unterdrückung von Essiggeruch |
Country Status (10)
Country | Link |
---|---|
US (1) | US8158178B2 (de) |
EP (2) | EP2000035A1 (de) |
JP (1) | JP5317301B2 (de) |
CN (1) | CN101715302B (de) |
BR (1) | BRPI0812139B1 (de) |
DK (1) | DK2166875T3 (de) |
ES (1) | ES2406421T3 (de) |
PL (1) | PL2166875T3 (de) |
PT (1) | PT2166875E (de) |
WO (1) | WO2008148848A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20210062413A (ko) | 2019-11-21 | 2021-05-31 | (주)아모레퍼시픽 | 고함량의 락테이트 금속염 및 실리콘계 오일의 혼합물을 포함하는 w/s형 화장료 조성물 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110060048A1 (en) * | 2009-09-05 | 2011-03-10 | Ashley Regina Lo | Removing alcohol in vivo through esterification |
US20130295230A1 (en) * | 2012-05-04 | 2013-11-07 | Nutraceutical Corporation | Sugar-free naturally preserved stevia supplement |
US10752871B2 (en) | 2012-08-01 | 2020-08-25 | Purac Biochem B.V. | Preparation of a powdered vinegar |
DK3660138T3 (da) | 2014-03-24 | 2023-06-06 | Purac Biochem Bv | Neutraliserede eddikekoncentrater og flydende blandinger af fødevarekvalitet med de neutraliserede eddikekoncentrater |
CA2942894C (en) * | 2014-03-24 | 2023-04-04 | Purac Biochem B.V. | Neutralized vinegar concentrates and liquid food grade blends containing said neutralized vinegar concentrates |
KR101742686B1 (ko) * | 2014-12-29 | 2017-06-01 | 샘표 주식회사 | 향미가 개선된 발효 식초 및 그 제조방법 |
CN105420062A (zh) * | 2016-01-13 | 2016-03-23 | 绿杰股份有限公司 | 一种消除果醋过强发酵风味的方法 |
CN106367303A (zh) * | 2016-08-31 | 2017-02-01 | 陈宇 | 一种苏打醋 |
WO2018056778A1 (ko) * | 2016-09-23 | 2018-03-29 | 샘표식품 주식회사 | 진주발효물을 포함하는 피부상태 개선용 조성물 |
CN106769601B (zh) * | 2016-12-12 | 2020-10-23 | 浙江农林大学 | 一种便捷测定木醋液中有机酸和木焦油的含量方法 |
CN106596324B (zh) * | 2016-12-12 | 2020-10-23 | 浙江农林大学 | 一种便捷测定竹醋液中有机酸和竹焦油的含量方法 |
EP3733782A4 (de) | 2017-12-28 | 2021-09-22 | Sekisui Chemical Co., Ltd. | Metallkomplexpartikel und reagenz für immunoassay damit |
WO2023100978A1 (ja) * | 2021-12-02 | 2023-06-08 | 株式会社Mizkan Holdings | 酢酸含有飲食品 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4833099A (de) * | 1971-09-06 | 1973-05-07 | ||
JPS5955163A (ja) * | 1982-09-21 | 1984-03-30 | Higeta Shoyu Kk | 食酢含有酸性液体調味料 |
JPH0632603B2 (ja) | 1983-12-26 | 1994-05-02 | 中外製薬株式会社 | 菌体付着異臭味成分の除去法 |
JPS60164475A (ja) * | 1984-02-03 | 1985-08-27 | Tamanoisu Kk | 醸造酢粉末の製法 |
JPS61227776A (ja) * | 1985-04-03 | 1986-10-09 | Nakano Vinegar Co Ltd | 食酢の製造方法 |
JPH0779660B2 (ja) | 1986-10-04 | 1995-08-30 | 株式会社リブ・インタ−ナシヨナル | 液状調味料の脱臭方法 |
JPS63137669A (ja) * | 1986-11-28 | 1988-06-09 | San Ei Chem Ind Ltd | 醸造酢の濃縮法 |
US4897272A (en) * | 1987-11-20 | 1990-01-30 | Tamanoi Vinegar Corporation Limited | Process for producing rice vinegar |
JPH01312990A (ja) * | 1988-06-11 | 1989-12-18 | Tamanoisu Kk | フェニル酢酸含量の少ない食酢及びその製造法 |
JPH02211859A (ja) * | 1989-02-09 | 1990-08-23 | Tamanoisu Kk | とうもろこしを原料とする食酢の精製法 |
US4994292A (en) | 1989-10-06 | 1991-02-19 | Tamanoi Vinegar Co., Ltd. | Process for the removal of iso-valeric acid from vinegar |
JPH0775543A (ja) * | 1993-09-09 | 1995-03-20 | Kikkoman Corp | 改良食酢の製造法およびその改良食酢を用いた食品 |
JPH10337167A (ja) * | 1997-06-05 | 1998-12-22 | Japan Organo Co Ltd | 食品の日持ち向上剤 |
JP3270732B2 (ja) * | 1997-12-22 | 2002-04-02 | 幸生 中野 | 梅果汁中のナトリウム濃度の低減方法、および梅果汁飲料の製造方法 |
JP4056905B2 (ja) * | 2003-02-28 | 2008-03-05 | 株式会社ミツカングループ本社 | 食酢飲料 |
ES2706178T3 (es) * | 2005-09-15 | 2019-03-27 | Triad Resource Tech Llc | Composiciones para mejorar el sabor y la seguridad en productos de carnes marinadas |
-
2007
- 2007-06-07 EP EP07109815A patent/EP2000035A1/de not_active Withdrawn
-
2008
- 2008-06-05 DK DK08760582.0T patent/DK2166875T3/da active
- 2008-06-05 PL PL08760582T patent/PL2166875T3/pl unknown
- 2008-06-05 CN CN2008800187519A patent/CN101715302B/zh active Active
- 2008-06-05 BR BRPI0812139-7A patent/BRPI0812139B1/pt active IP Right Grant
- 2008-06-05 EP EP08760582A patent/EP2166875B1/de active Active
- 2008-06-05 JP JP2010510805A patent/JP5317301B2/ja active Active
- 2008-06-05 ES ES08760582T patent/ES2406421T3/es active Active
- 2008-06-05 WO PCT/EP2008/057006 patent/WO2008148848A1/en active Application Filing
- 2008-06-05 PT PT87605820T patent/PT2166875E/pt unknown
- 2008-06-05 US US12/155,517 patent/US8158178B2/en active Active
Non-Patent Citations (1)
Title |
---|
See references of WO2008148848A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20210062413A (ko) | 2019-11-21 | 2021-05-31 | (주)아모레퍼시픽 | 고함량의 락테이트 금속염 및 실리콘계 오일의 혼합물을 포함하는 w/s형 화장료 조성물 |
Also Published As
Publication number | Publication date |
---|---|
CN101715302A (zh) | 2010-05-26 |
ES2406421T3 (es) | 2013-06-06 |
DK2166875T3 (da) | 2013-05-13 |
CN101715302B (zh) | 2013-10-02 |
BRPI0812139B1 (pt) | 2017-12-12 |
JP2010528640A (ja) | 2010-08-26 |
EP2166875B1 (de) | 2013-02-27 |
US8158178B2 (en) | 2012-04-17 |
JP5317301B2 (ja) | 2013-10-16 |
US20080305228A1 (en) | 2008-12-11 |
PL2166875T3 (pl) | 2013-08-30 |
WO2008148848A1 (en) | 2008-12-11 |
PT2166875E (pt) | 2013-05-21 |
BRPI0812139A2 (pt) | 2014-09-30 |
EP2000035A1 (de) | 2008-12-10 |
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